Science · 2004 · 477 citations · 27 references
Life SciencesGeneticsMolecular BiologyGene ExpressionGene TherapyRna ProcessingMuscle PathologyMuscular DystrophyProtein SynthesisRna EditingRna InterferenceAntisense RnasAntisense TranscriptionEditing For Muscular DystrophyExon SkippingExon Skipping TherapyMuscular Dystrophy PathophysiologyPhysiological CharacterizationSmall Nuclear Rna Genes
Most mutations in the dystrophin gene create a frameshift or a stop in the mRNA and are associated with severe Duchenne muscular dystrophy. Exon skipping that naturally occurs at low frequency sometimes eliminates the mutation and leads to the production of a rescued protein. We have achieved persistent exon skipping that removes the mutated exon on the dystrophin messenger mRNA of the mdx mouse, by a single administration of an AAV vector expressing antisense sequences linked to a modified U7 small nuclear RNA. We report the sustained production of functional dystrophin at physiological levels in entire groups of muscles and the correction of the muscular dystrophy.
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The Molecular Basis of Muscular Dystrophy in the <i>mdx</i> Mouse: a Point Mutation
Piotr Siciński, Yan Geng, Allan S. Ryder-Cook et al. · Science · 1989 · 1.2K citations
A compensatory base change in U1 snRNA suppresses a 5′ splice site mutation
Yuan Zhuang, Alan M. Weiner · Cell · 1986 · 761 citations
AAV-mediated factor IX gene transfer to skeletal muscle in patients with severe hemophilia B
Catherine S. Manno, Ah Keng Chew, S Hutchison et al. · Blood · 2003 · 747 citations · Full text
Medicine, Genetics, Hematology +11